DIN EN ISO 11607-1:2017-10
Withdrawn
View Superseded by
Packaging for terminally sterilized medical devices – Part 1: Requirements for materials, sterile barrier systems and packaging systems (ISO 116071: 2006 + Amd 1:2014); English version EN ISO 116071: 2017, English translation of DIN EN ISO 11607-1:2017-10
Hardcopy , PDF
English
10-01-2017
01-30-2021
This part of ISO 11607 specifies the requirements and test methods for materials, preformed sterile barrier systems, sterile barrier systems and packaging systems that are intended to maintain sterility of terminally sterilized medical devices until the point of use.
| Committee |
TC 198
|
| DocumentType |
Test Method
|
| Pages |
0
|
| ProductNote |
This Standard also refers to:EN 868-5:1999,EN 868-6:2009,EN 868-7:2009,EN 868-8:1999,EN 868-9:2000,EN 868-10:2000,EN 1422:1997,EN 14180+A2:2009,AAMI/ANSI ST 65:2008.
|
| PublisherName |
German Institute for Standardisation (Deutsches Institut für Normung)
|
| Status |
Withdrawn
|
| SupersededBy | |
| Supersedes |
| Standards | Relationship |
| EN ISO 11607-1:2017 | Identical |
| ISO 11607-1:2006/Amd 1:2014 | Identical |
| I.S. EN ISO 11607-1:2017 | Equivalent |
| BS EN ISO 11607-1:2017 | Equivalent |
| UNE-EN ISO 11607-1:2017 | Equivalent |
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